A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872001



Internal ID22646939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14084..226386hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38212303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872001
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer